KIF20B

kinesin family member 20B

Summary

Enables several functions, including ATP hydrolysis activity; WW domain binding activity; and plus-end-directed microtubule motor activity. Involved in positive regulation of cell population proliferation and positive regulation of cytokinesis. Located in several cellular components, including microtubule cytoskeleton; midbody; and nuclear lumen. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants105 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs753159710	10:91,465,132	A/T	—	uncertain significance
rs2492907962	10:91,465,146	G/A	—	uncertain significance
rs148065279	10:91,465,167	A/G	—	likely benign
rs367726513	10:91,468,948	T/C	—	uncertain significance
rs375851858	10:91,468,955	A/C	—	uncertain significance
rs372714100	10:91,469,693	C/T	—	uncertain significance
rs140764762	10:91,469,697	C/T	—	uncertain significance
rs771970019	10:91,469,706	A/G	—	uncertain significance
rs149777607	10:91,469,729	A/G	—	uncertain significance
rs374626048	10:91,469,732	A/G	—	uncertain significance
rs368664005	10:91,469,768	C/T	—	uncertain significance
rs372770283	10:91,469,786	G/A	—	uncertain significance
rs764335006	10:91,470,792	A/G	—	uncertain significance
rs12414269	10:91,474,539	G/A	intron variant	—
rs201019984	10:91,474,825	T/G	—	uncertain significance
rs748115970	10:91,476,234	A/G	—	uncertain significance
rs367763475	10:91,476,265	G/A	—	uncertain significance
rs2492940475	10:91,476,267	G/A	—	uncertain significance
rs140162687	10:91,477,337	T/A	—	benign
rs149456198	10:91,477,454	G/A	—	uncertain significance
rs1050818241	10:91,478,615	G/A	—	uncertain significance
rs147397224	10:91,479,192	C/G	—	uncertain significance
rs150845034	10:91,479,272	A/G	—	uncertain significance
rs1843008708	10:91,479,408	A/C	—	uncertain significance
rs373446473	10:91,479,414	A/T	—	uncertain significance
rs2492960911	10:91,483,785	C/A	—	uncertain significance
rs779990837	10:91,484,799	G/A	—	uncertain significance
rs375544106	10:91,484,823	C/T	—	likely benign
rs755409283	10:91,484,826	C/T	—	uncertain significance
rs1206034890	10:91,484,844	G/C	—	uncertain significance
rs2492964910	10:91,484,850	G/A	—	uncertain significance
rs145716217	10:91,484,881	C/T	—	uncertain significance
rs184189311	10:91,486,076	A/G	—	likely benign
rs748647932	10:91,486,176	A/G	—	uncertain significance
rs771063788	10:91,486,205	A/C	—	uncertain significance
rs183238428	10:91,486,253	A/T	—	uncertain significance
rs762501126	10:91,488,907	G/T	—	uncertain significance
rs147005975	10:91,488,951	A/G	—	uncertain significance
rs373615206	10:91,488,957	G/A	—	likely benign
rs1394768783	10:91,488,988	A/T	—	uncertain significance
rs1297694740	10:91,492,757	A/C	—	uncertain significance
rs3925446	10:91,495,322	G/A	intron variant	—
rs762003553	10:91,497,155	G/T	—	uncertain significance
rs777512294	10:91,497,204	C/T	—	uncertain significance
rs78963463	10:91,497,207	A/G	—	benign
rs375340649	10:91,497,210	T/C	—	uncertain significance
rs765334220	10:91,497,227	A/C	—	uncertain significance
rs938519006	10:91,497,244	A/C	—	uncertain significance
rs372813515	10:91,497,276	C/T	—	likely benign
rs2492998077	10:91,497,288	A/G	—	uncertain significance
rs1302020036	10:91,497,423	T/C	—	uncertain significance
rs147780471	10:91,497,562	A/C	—	uncertain significance
rs768593820	10:91,497,567	A/G	—	uncertain significance
rs373614828	10:91,497,571	A/T	—	uncertain significance
rs34999049	10:91,497,605	A/G	—	likely benign
rs745947393	10:91,497,612	A/C	—	uncertain significance
rs2493000404	10:91,497,785	G/A	—	uncertain significance
rs2133128057	10:91,497,957	T/C	—	uncertain significance
rs368304916	10:91,497,960	T/G	—	uncertain significance
rs1366788261	10:91,498,013	A/G	—	likely benign
rs775642819	10:91,498,040	G/A	—	uncertain significance
rs2493002117	10:91,498,137	C/T	—	likely benign
rs2493002237	10:91,498,158	T/C	—	uncertain significance
rs772928928	10:91,498,167	A/C	—	uncertain significance
rs2493002507	10:91,498,205	G/A	—	uncertain significance
rs144980311	10:91,498,229	T/C	—	uncertain significance
rs147115055	10:91,498,232	G/A	—	likely benign
rs751880293	10:91,498,310	G/A	—	uncertain significance
rs35663373	10:91,498,730	C/T	—	benign
rs757329358	10:91,498,744	C/T	—	uncertain significance
rs372651065	10:91,498,778	G/C	—	uncertain significance
rs376129504	10:91,503,577	C/T	—	uncertain significance
rs751875487	10:91,503,633	C/T	—	likely benign
rs143200257	10:91,503,652	G/T	—	uncertain significance
rs777798374	10:91,503,665	G/A	—	uncertain significance
rs77291744	10:91,505,334	T/A	intron variant	—
rs76785586	10:91,505,704	A/C	—	benign
rs1326201	10:91,510,982	T/C	intron variant	—
rs139452485	10:91,511,198	A/C	—	uncertain significance
rs149758232	10:91,512,341	G/A	—	uncertain significance
rs772928845	10:91,512,371	A/T	—	uncertain significance
rs2493041410	10:91,512,393	A/C	—	uncertain significance
rs145399222	10:91,512,410	G/T	—	uncertain significance
rs768347589	10:91,514,323	A/G	—	uncertain significance
rs372720193	10:91,514,343	A/T	—	uncertain significance
rs753954878	10:91,514,345	C/T	—	uncertain significance
rs1330526853	10:91,514,401	G/C	—	uncertain significance
rs763688811	10:91,514,405	G/A	—	uncertain significance
rs543186692	10:91,518,502	C/G	—	uncertain significance
rs769017488	10:91,518,566	T/C	—	uncertain significance
rs777231047	10:91,518,568	A/C	—	uncertain significance
rs1842184309	10:91,518,637	A/G	—	uncertain significance
rs568916589	10:91,519,234	C/A	—	—
rs773387834	10:91,520,292	A/G	—	uncertain significance
rs1400076532	10:91,520,340	C/T	—	uncertain significance
rs764084518	10:91,522,414	A/T	—	uncertain significance
rs751324087	10:91,522,444	A/G	—	uncertain significance
rs2493067159	10:91,522,486	C/T	—	uncertain significance
rs1348969834	10:91,522,552	T/A	—	uncertain significance
rs1015551557	10:91,528,086	A/G	—	uncertain significance

Showing 100 of 105 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.